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SASKATOON, Canada — Crestline Coach is so pleased to be part of a true Saskatchewan Collaboration, "2016 Drive for Kids Campaign". In partnership with Synergy 8, the Children's Hospital Foundation of Saskatchewan, the Sandra Schmirler Foundation and many other sponsors a fully customized, state-of-the-art Pediatric Ambulance was designed and built for the province of Saskatchewan ...
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The most common cause of jaundice during pregnancy in the United States (US) is still attributed to viral hepatitis, despite the dramatic drop in incidence of viral hepatitis in the US.
We hypothesized that viral hepatitis is no longer a frequent etiology of jaundice among the pregnant population in the US and sought to identify the contemporary causes of elevated bilirubin during pregnancy as well as to quantify the associated risk to the mother and fetus.
Clinical data from all pregnant women who delivered an infant between 2005 and 2011 at a single hospital in Dallas, Texas, were ascertained using prospectively collected computerized databases. Women with elevated total bilirubin (>1.2 mg/dl) were analyzed to determine the cause of hyperbilirubinemia and maternal and fetal outcomes.
Out of a total of 80,857 consecutive deliveries, there were 397 (0.5 %) pregnancies with hyperbilirubinemia. The most common etiology was gallstones (98/397 = 25 %), followed by preeclampsia/eclampsia/HELLP (94/397 = 24 %) and intrahepatic cholestasis of pregnancy (53/397 = 13 %). Adverse infant outcomes, including stillbirths, fetal malformations, neonatal deaths, and small for gestational age births, were more common in the women with hyperbilirubinemia during pregnancy, but there were no maternal deaths.
Acute viral hepatitis is no longer a common cause of jaundice in pregnant women in the US. In the current era, gallstones and preeclampsia-related disorders are the most common causes of jaundice in pregnant women. Disorders that cause elevated maternal bilirubin during pregnancy are associated with increased risk for the fetus.
The treatment of non-metastatic rectal cancer has been instated in the past century based on the validation of the chemo-radiotherapy in a neo-adjuvant setting. The incidence of rectal cancer is around 39.000 new cases per year in the United States [1]. The probability of survival at 3 years is approximately 85% with a cumulative incidence of local recurrence about 5% [2]. Treatment is based on the surgical resection with a total meso-rectal excision associated with a preoperative radio-chemotherapy.
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The North American Spine Society's (NASS) Evidence-Based Clinical Guideline for the Diagnosis and Treatment of Adult Isthmic Spondylolisthesis features evidence-based recommendations for diagnosing and treating adult patients with isthmic spondylolisthesis. The guideline is intended to reflect contemporary treatment concepts for symptomatic isthmic spondylolisthesis as reflected in the highest quality clinical literature available on this subject as of June 2013. NASS' guideline on this topic is the only guideline on adult isthmic spondylolisthesis accepted in the Agency for Healthcare Research and Quality's National Guideline Clearinghouse.
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Lumbar axial back pain arising from degenerative disc disease continues to be a challenging clinical problem whether treated with non-surgical management, local injection, or motion segment stabilization and fusion.
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The treatment of non-metastatic rectal cancer has been instated in the past century based on the validation of the chemo-radiotherapy in a neo-adjuvant setting. The incidence of rectal cancer is around 39.000 new cases per year in the United States [1]. The probability of survival at 3 years is approximately 85% with a cumulative incidence of local recurrence about 5% [2]. Treatment is based on the surgical resection with a total meso-rectal excision associated with a preoperative radio-chemotherapy.
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Publication date: Available online 1 September 2016
Source:Archives of Physical Medicine and Rehabilitation
Author(s): Feng-Hang Chang, Tsan-Hon Liou, Pengsheng Ni, Kwang-Hwa Chang, Chien-Hung Lai
ObjectiveTo describe the development of a participation measure that assesses three domains (productivity, social, and community) and four dimensions (frequency, diversity, desire for change, and perceived difficulty) of participation and to evaluate the initial psychometric properties in rehabilitation outpatients.DesignA mixed-method approach included a literature review, item selection, expert reviews, cognitive interviews and field testing with rehabilitation outpatients. A confirmatory factor analysis (CFA) and Rasch analysis were used to validate the construct validity of the difficulty dimension of the instrument.SettingOutpatient rehabilitation programs in Taiwan.ParticipantsAn expert panel consisting of 12 rehabilitation and measurement experts contributed to measurement development; 20 rehabilitation outpatients participated in cognitive interviews; and 556 rehabilitation outpatients (with an average age of 61.36±23.62 years, among whom 53% were male) participated in field testing.Main outcome measureThe Participation Measure--3 Domains, 4 Dimensions (PM-3D4D).ResultsA scoring method for each dimension of the PM-3D4D was established. The instrument displayed good overall model fit in the CFA and unidimensionality across three domains after removing and collapsing locally dependent items identified from a principal component analysis (PCA). However, considering the poor personal reliability of the social subscale and its high correlation with the community subscale, we decided to merge the two subscales into one. The combined subscale showed improved reliability and good construct validity by demonstrating a good model fit (CFI =0.985, TLI =0.982, RMSEA =0.061) and item fit.ConclusionsThe PM-3D4D is a newly developed participation measure designed to assess multiple domains and dimensions of participation by rehabilitation patients. The psychometric analysis results supported the construct of the instrument and helped item revision. Further examination of the validity and reliability of the PM-3D4D will be conducted.
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By EMS1 Staff
FARGO, N.D. — Two paramedics with F-M Ambulance were recognized for outstanding acts of bravery in the line of duty.
Wednesday's ceremony marked the first time the agency has ever awarded the Medal of Valor, which can only be earned in extraordinary circumstances.
F-M Ambulance Director Sherm Syverson told WDAY TV that it's hard to talk about the specific events leading up to the awards, but confirmed that the paramedics risked their lives in the face of danger to provide care.
Greg Glood, who was off-duty at the time, ran into a burning house to help a person trapped inside. Glood prevented bystanders from entering the house and stayed on scene until ambulances arrived to help treat the patient's injuries.
Kelsey Bodvig responded to an armed standoff as part of the Red River Valley SWAT Tactical EMS team. She provided lifesaving care to a team member at the scene
WDAY reports that both medics served in the U.S. military, and Bodvig will deploy to Kuwait in the coming months.
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In this week's episode of Inside EMS, co-hosts Chris Cebollero and Kelly Grayson discuss the ever-persistent issue of unprofessional behavior in the EMS world. The two offer advice on how to deal with a difficult partner, how to properly begin difficult discussions and how to decrease egotism.
Archives of Medical Science
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Journal of Clinical Microbiology
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Annals of Allergy, Asthma, and Immunology
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Histopathology
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Transplantation Proceedings
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Journal of Digestive Diseases
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International Journal of Obesity
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BMC Pediatrics
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International Journal of Obesity
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World Journal of Emergency Surgery
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The tenascin-X (TNX) deficient type Ehlers-Danlos syndrome (EDS) is similar to the classical type of Ehlers-Danlos syndrome. Due to the limited awareness among geneticists and the challenge of the molecular analysis of the TNXB gene, the TNX-deficient type EDS is likely to be under diagnosed. We therefore performed an observational, cross-sectional study. History and physical examination were performed. Results of serum TNX measurements were collected and mutation analysis was performed by a combination of NGS, Sanger sequencing and MLPA. Included were 17 patients of 11 families with autosomal recessive inheritance and childhood onset. All patients had hyperextensible skin without atrophic scarring. Hypermobility of the joints was observed in 16/17 patients. Deformities of the hands and feet were observed frequently. TNX serum level was tested and absent in 11 patients (7 families). Genetic testing was performed in all families; 12 different mutations were detected, most of which are suspected to lead to non-sense mRNA mediated decay. In short, patients with the TNX-deficient type EDS typically have generalized joint hypermobility, skin hyperextensibility and easy bruising. In contrast to the classical type, the inheritance pattern is autosomal recessive and atrophic scarring is absent. Molecular analysis of TNXB in a diagnostic setting is challenging.